Odaguchi Hiroshi, Hyuga Sumiko, Sekine Mariko, Michimae Hirofumi, Hyuga Masashi, Uchiyama Nahoko, Uema Masashi, Kumagai Yuji, Suzuki Yusuke, Nabeshima Shigeki, Omagari Norio, Doi Yohei, Yamaoka Kunihiro, Miyazaki Koji, Fuji Susumu, Umezawa Yoshihiro, Kodera Shiho, Nagashima Hirotaka, Hirose Wataru, Goda Yukihiro
Oriental Medicine Research Center, School of Pharmacy, Kitasato University, Tokyo108-8641, Japan.
Kitasato University Kitasato Institute Hospital, Shirokane Campus, Tokyo 108-8642, Japan.
Microorganisms. 2025 Mar 12;13(3):641. doi: 10.3390/microorganisms13030641.
Several Ephedra Herb-containing Kampo medicines are common initial treatments for various infections; however, the ephedrine alkaloids in Ephedra Herb can cause side effects by stimulating adrenergic receptors. Accordingly, an ephedrine alkaloids-free Ephedra Herb Extract (EFE) has been developed. This study aimed to evaluate whether EFE can be used effectively and safely in patients with mild coronavirus disease 2019 (COVID-19). We randomized patients with mild COVID-19 to receive EFE equivalent to 6 g of Ephedra Herb per day or a placebo for 14 days. The primary efficacy endpoint was the non-aggravation rate up to Day 15. We allocated 41 and 40 patients to the EFE and placebo groups, respectively. All participants were included in the mITT and safety analysis populations [male ratio, mean age: 31.7%, 42.0 years (EFE); 17.5%, 43.2 years (placebo)]. The non-aggravation rate up to Day 15 for the primary endpoint was 100.0% and 94.6% in the EFE and placebo group, respectively, with no between-group difference. The number of days to the improvement in nausea symptoms was significantly shorter in the EFE group. One patient in the placebo group discontinued the trial due to a side effect. Although EFE demonstrated safety in patients with mild COVID-19, it did not show superior efficacy compared to placebo for symptoms other than nausea.
几种含麻黄的汉方药是治疗各种感染的常见初始疗法;然而,麻黄中的麻黄碱生物碱可通过刺激肾上腺素能受体引起副作用。因此,已开发出一种无麻黄碱生物碱的麻黄提取物(EFE)。本研究旨在评估EFE在轻度2019冠状病毒病(COVID-19)患者中能否有效且安全地使用。我们将轻度COVID-19患者随机分组,分别给予相当于每天6克麻黄的EFE或安慰剂,为期14天。主要疗效终点是至第15天的病情无加重率。我们分别将41例和40例患者分配至EFE组和安慰剂组。所有参与者均纳入意向性分析(mITT)和安全性分析人群[男性比例、平均年龄:31.7%,42.0岁(EFE组);17.5%,43.2岁(安慰剂组)]。主要终点至第15天的病情无加重率在EFE组和安慰剂组分别为100.0%和94.6%,组间无差异。EFE组恶心症状改善天数显著更短。安慰剂组有1例患者因副作用而停止试验。虽然EFE在轻度COVID-19患者中显示出安全性,但对于除恶心之外的症状,其疗效并不优于安慰剂。